What are the responsibilities and job description for the Associate Quality Control I - West Greenwich, RI position at VetJobs?
Job Description
ATTENTION MILITARY AFFILIATED JOB SEEKERS - Our organization works with partner companies to source qualified talent for their open roles. The following position is available to Veterans, Transitioning Military, National Guard and Reserve Members, Military Spouses, Wounded Warriors, and their Caregivers. If you have the required skill set, education requirements, and experience, please click the submit button and follow the next steps. Unless specifically stated otherwise, this role is "On-Site" at the location detailed in the job post.
Quality Control Associate - Bioanalytics
What you will do
Let’s do this. Let’s change the world. In this vital role you will complete and review analytical testing in our cGMP laboratory. The role will be on-site based out of Amgen Rhode Island and will work under the mentorship of the front-line manager. The Bioanalytics team provides analytical expertise in testing the following: in-process, release and stability samples. The laboratory employs a variety of test methodologies that use sophisticated equipment including: HPLC/UPLC, capillary electrophoresis and general chemistry methodologies such as: Appearance, Color, Clarity, pH, Osmolality, Polysorbate, Protein Concentration, and Sub-Visible Particle testing.
Responsibilities Include The Following
Follow safety guidelines, cGMPs (Good Manufacturing Practices) and other applicable regulatory requirements
Generate complete, accurate, and concise laboratory documentation using electronic systems and laboratory notebooks
Ensures that facilities, equipment, materials, organization, processes, procedures and products follow cGMP practices and other applicable regulations
Operate laboratory equipment and instrumentation
Performs review and approval of assays, documents and records
Supports Continual Improvement initiatives
Alerts management of quality, compliance, supply and safety risks
Participate in laboratory investigations
Perform general laboratory housekeeping activities
Completes required assigned training to permit carry through of required tasks
Performs additional duties as specified by management
Auto req ID
468528BR
Minimum Education Required
High School/GED
Job_Category
Manufacturing
Additional Qualifications/Responsibilities
What we expect of you
We are all different, yet we all use our unique contributions to serve patients. The experienced professional we seek thrives in a fast-paced environment and possesses these qualifications.
Basic Qualifications
High school diploma/GED and 2 years of Quality experience OR
Associate's degree and 6 months of Quality experience OR
Bachelor's Degree
Preferred Qualifications
1-2 years’ experience in HPLC/UPLC, capillary electrophoresis and general chemistry methodologies such as: Appearance, Color, Clarity, pH, Osmolality, Polysorbate, Protein Concentration, and Sub-Visible Particle testing
Demonstrated experience in laboratory investigations, method validation, audits, QC processes
Proven ability to interpret scientific data
Self-motivated, strong organizational skills and ability to manage multiple tasks at one time with minimal direction
Strong communication skills (both written and oral), facilitation and presentation skills
GMP/GDP experience
What you can expect of us
As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way.
The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications.
In Addition To The Base Salary, Amgen Offers a Total Rewards Plan, Based On Eligibility, Comprising Of Health And Welfare Plans For Staff And Eligible Dependents, Financial Plans With Opportunities To Save Towards Retirement Or Other Goals, Work/life Balance, And Career Development Opportunities That May Include
A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts
A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
Stock-based long-term incentives
Award-winning time-off plans
Flexible work models where possible. Refer to the Work Location Type in the job posting to see if this applies.
Apply now and make a lasting impact with the Amgen team.
Salary Range
66,222.00 USD - 82,012.00 USD
City*
West Greenwich
State*
Rhode Island
Job Code
Pharmaceutical Pharmaceutical
Affiliate Sponsor
Amgen
Salary Range
$75,000-$100,000
ATTENTION MILITARY AFFILIATED JOB SEEKERS - Our organization works with partner companies to source qualified talent for their open roles. The following position is available to Veterans, Transitioning Military, National Guard and Reserve Members, Military Spouses, Wounded Warriors, and their Caregivers. If you have the required skill set, education requirements, and experience, please click the submit button and follow the next steps. Unless specifically stated otherwise, this role is "On-Site" at the location detailed in the job post.
Quality Control Associate - Bioanalytics
What you will do
Let’s do this. Let’s change the world. In this vital role you will complete and review analytical testing in our cGMP laboratory. The role will be on-site based out of Amgen Rhode Island and will work under the mentorship of the front-line manager. The Bioanalytics team provides analytical expertise in testing the following: in-process, release and stability samples. The laboratory employs a variety of test methodologies that use sophisticated equipment including: HPLC/UPLC, capillary electrophoresis and general chemistry methodologies such as: Appearance, Color, Clarity, pH, Osmolality, Polysorbate, Protein Concentration, and Sub-Visible Particle testing.
Responsibilities Include The Following
Follow safety guidelines, cGMPs (Good Manufacturing Practices) and other applicable regulatory requirements
Generate complete, accurate, and concise laboratory documentation using electronic systems and laboratory notebooks
Ensures that facilities, equipment, materials, organization, processes, procedures and products follow cGMP practices and other applicable regulations
Operate laboratory equipment and instrumentation
Performs review and approval of assays, documents and records
Supports Continual Improvement initiatives
Alerts management of quality, compliance, supply and safety risks
Participate in laboratory investigations
Perform general laboratory housekeeping activities
Completes required assigned training to permit carry through of required tasks
Performs additional duties as specified by management
Auto req ID
468528BR
Minimum Education Required
High School/GED
Job_Category
Manufacturing
Additional Qualifications/Responsibilities
What we expect of you
We are all different, yet we all use our unique contributions to serve patients. The experienced professional we seek thrives in a fast-paced environment and possesses these qualifications.
Basic Qualifications
High school diploma/GED and 2 years of Quality experience OR
Associate's degree and 6 months of Quality experience OR
Bachelor's Degree
Preferred Qualifications
1-2 years’ experience in HPLC/UPLC, capillary electrophoresis and general chemistry methodologies such as: Appearance, Color, Clarity, pH, Osmolality, Polysorbate, Protein Concentration, and Sub-Visible Particle testing
Demonstrated experience in laboratory investigations, method validation, audits, QC processes
Proven ability to interpret scientific data
Self-motivated, strong organizational skills and ability to manage multiple tasks at one time with minimal direction
Strong communication skills (both written and oral), facilitation and presentation skills
GMP/GDP experience
What you can expect of us
As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way.
The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications.
In Addition To The Base Salary, Amgen Offers a Total Rewards Plan, Based On Eligibility, Comprising Of Health And Welfare Plans For Staff And Eligible Dependents, Financial Plans With Opportunities To Save Towards Retirement Or Other Goals, Work/life Balance, And Career Development Opportunities That May Include
A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts
A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
Stock-based long-term incentives
Award-winning time-off plans
Flexible work models where possible. Refer to the Work Location Type in the job posting to see if this applies.
Apply now and make a lasting impact with the Amgen team.
Salary Range
66,222.00 USD - 82,012.00 USD
City*
West Greenwich
State*
Rhode Island
Job Code
Pharmaceutical Pharmaceutical
Affiliate Sponsor
Amgen
Salary Range
$75,000-$100,000
Salary : $75,000 - $100,000